减少四级新生儿重症监护室中与早产儿相关骨折的骨质疏松:质量改进计划。

IF 1.2 Q3 PEDIATRICS Pediatric quality & safety Pub Date : 2024-04-03 eCollection Date: 2024-03-01 DOI:10.1097/pq9.0000000000000723
Linsey Cromwell, Katherine Breznak, Megan Young, Anoosha Kasangottu, Sharon Leonardo, Catherine Markel, Andreea Marinescu, Folasade Kehinde, Vilmaris Quinones Cardona
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引用次数: 0

摘要

背景:早产儿骨质疏松症(OOP早产儿骨质疏松症(OOP)通常是新生儿重症监护室(NICU)中的一种隐性疾病。尽管早产儿骨质疏松与新生儿骨折等发病率增加有关,但筛查、诊断和管理方法却存在很大差异。我们的目标是在一年内将四级新生儿重症监护病房中与 OOP 相关的骨折发生率降低 20%:一个多学科质量改进小组发现,OOP 筛选、诊断和管理的不一致以及对高危患者的处理是导致 OOP 相关骨折的主要原因。利用改进模型,我们实施了一系列干预措施,包括筛查、诊断和管理算法,将其作为 "护理处理 "捆绑包,用于处理有骨折风险的婴儿:共纳入 194 名高风险婴儿,其中 59 名患有 OOP。与 OOP 相关的骨折有特殊原因,在我们的干预下,骨折率从每 1000 个住院日 0.43 例降至每 1000 个住院日 0.06 例。骨折间隔天数也从 62 天减少到 337 天。尽管在整个行动中,OOP 的发生率相似,但我们还是取得了这些进步。我们发现了一些特殊原因导致的差异,如遗漏 OOP 记录的患者增多,以及在出生后 4 周收集 OOP 筛查实验室数据的情况有所改善,但血液检测并未增加:多学科团队采用标准化的 OOP 筛查、诊断和管理指南(包括护理捆绑包),减少了 IV 级新生儿重症监护病房中与 OOP 相关的骨折。
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Reducing Osteopenia of Prematurity-related Fractures in a Level IV NICU: A Quality Improvement Initiative.

Background: Osteopenia of prematurity (OOP) is often a silent disease in the neonatal intensive care unit (NICU). Despite its association with increased neonatal morbidity, such as fractures, wide variation exists in screening, diagnostic, and management practices. We sought to decrease the rate of OOP-related fractures in our level IV NICU by 20% within 1 year.

Methods: A multidisciplinary quality improvement team identified inconsistent screening, diagnosis, and management of OOP, as well as handling of at-risk patients, as primary drivers for OOP-related fractures. Using the model for improvement, we implemented sequential interventions, including screening, diagnosis, and a management algorithm as a "handle-with-care" bundle in infants at risk for fractures.

Results: 194 at-risk infants were included, 59 of whom had OOP. There was special cause variation in OOP-related fractures, with a reduction from 0.43 per 1000 patient days to 0.06 per 1000 patient days with our interventions. There was also an improvement in days between fractures from 62 to 337 days. We achieved these improvements despite a similar prevalence of OOP throughout the initiative. We showed special cause variation with increased patients between missed OOP documentation and improved collection of OOP screening laboratories at 4 weeks of life without increased blood testing.

Conclusion: A multidisciplinary team approach with standardized OOP screening, diagnosis, and management guidelines, including a handle-with-care bundle, reduces OOP-related fractures in a level IV NICU.

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CiteScore
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20 weeks
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